Clinical Trial Site Manager & Study Oversight CRA

Tigermed; Nantes; Sur place; EUR 45 000 - 60 000; Plein temps

Résumé du poste

A leading clinical research organization in Nantes is seeking a Clinical Research Associate. This role involves project management for clinical studies, ensuring high data quality, and compliance with regulations. The ideal candidate will have at least 2 years of CRA experience, knowledge of Good Clinical Practice, and a bachelor's degree in biomedical sciences. Proficiency in Microsoft Office tools and strong communication skills are required. This position offers an opportunity to contribute to impactful clinical research in a collaborative environment.

Qualifications

• At least 2 years of CRA experience.
• Experience in at least 3 medical device clinical trials.
• Good written and oral English.

Responsabilités

• Manage all aspects of assigned clinical studies from initiation to close-out.
• Conduct monitoring visits according to the monitoring plan.
• Ensure timely collection of essential documents and study records.

Connaissances

Understanding of Good Clinical Practice

Team collaboration

Communication skills

Information-gathering skills

Formation

Bachelor degree in biomedical / medical science

Outils

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Description du poste

A leading clinical research organization in Nantes is seeking a Clinical Research Associate. This role involves project management for clinical studies, ensuring high data quality, and compliance with regulations. The ideal candidate will have at least 2 years of CRA experience, knowledge of Good Clinical Practice, and a bachelor's degree in biomedical sciences. Proficiency in Microsoft Office tools and strong communication skills are required. This position offers an opportunity to contribute to impactful clinical research in a collaborative environment.